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Circulating Tumor Cells in Right- and Left-Sided Colorectal Cancer
Molecular alterations are not randomly distributed in colorectal cancer (CRC), but rather clustered on the basis of primary tumor location underlying the importance of colorectal cancer sidedness. We aimed to investigate whether circulating tumor cells (CTC) characterization might help clarify how d...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721440/ https://www.ncbi.nlm.nih.gov/pubmed/31344798 http://dx.doi.org/10.3390/cancers11081042 |
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author | Nicolazzo, Chiara Raimondi, Cristina Gradilone, Angela Emiliani, Alessandra Zeuner, Ann Francescangeli, Federica Belardinilli, Francesca Seminara, Patrizia Loreni, Flavia Magri, Valentina Tomao, Silverio Gazzaniga, Paola |
author_facet | Nicolazzo, Chiara Raimondi, Cristina Gradilone, Angela Emiliani, Alessandra Zeuner, Ann Francescangeli, Federica Belardinilli, Francesca Seminara, Patrizia Loreni, Flavia Magri, Valentina Tomao, Silverio Gazzaniga, Paola |
author_sort | Nicolazzo, Chiara |
collection | PubMed |
description | Molecular alterations are not randomly distributed in colorectal cancer (CRC), but rather clustered on the basis of primary tumor location underlying the importance of colorectal cancer sidedness. We aimed to investigate whether circulating tumor cells (CTC) characterization might help clarify how different the patterns of dissemination might be relative to the behavior of left- (LCC) compared to right-sided (RCC) cancers. We retrospectively analyzed patients with metastatic CRC who had undergone standard baseline CTC evaluation before starting any first-line systemic treatment. Enumeration of CTC in left- and right-sided tumors were compared. The highest prognostic impact was exerted by CTC in left-sided primary cancer patients, even though the lowest median number of cells was detected in this subgroup of patients. CTC exhibit phenotypic heterogeneity, with a predominant mesenchymal phenotype found in CTC from distal compared to proximal primary tumors. Most CTC in RCC patients exhibited an apoptotic pattern. CTC in left-sided colon cancer patients exhibit a predominant mesenchymal phenotype. This might imply a substantial difference in the biology of proximal and distal cancers, associated with different patterns of tumor cells dissemination. The poor prognosis of right-sided CRC is not determined by the hematogenous dissemination of tumor cells, which appears to be predominantly a passive shedding of non-viable cells. Conversely, the subgroup of poor-prognosis left-sided CRC is reliably identified by the presence of mesenchymal CTC. |
format | Online Article Text |
id | pubmed-6721440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67214402019-09-10 Circulating Tumor Cells in Right- and Left-Sided Colorectal Cancer Nicolazzo, Chiara Raimondi, Cristina Gradilone, Angela Emiliani, Alessandra Zeuner, Ann Francescangeli, Federica Belardinilli, Francesca Seminara, Patrizia Loreni, Flavia Magri, Valentina Tomao, Silverio Gazzaniga, Paola Cancers (Basel) Article Molecular alterations are not randomly distributed in colorectal cancer (CRC), but rather clustered on the basis of primary tumor location underlying the importance of colorectal cancer sidedness. We aimed to investigate whether circulating tumor cells (CTC) characterization might help clarify how different the patterns of dissemination might be relative to the behavior of left- (LCC) compared to right-sided (RCC) cancers. We retrospectively analyzed patients with metastatic CRC who had undergone standard baseline CTC evaluation before starting any first-line systemic treatment. Enumeration of CTC in left- and right-sided tumors were compared. The highest prognostic impact was exerted by CTC in left-sided primary cancer patients, even though the lowest median number of cells was detected in this subgroup of patients. CTC exhibit phenotypic heterogeneity, with a predominant mesenchymal phenotype found in CTC from distal compared to proximal primary tumors. Most CTC in RCC patients exhibited an apoptotic pattern. CTC in left-sided colon cancer patients exhibit a predominant mesenchymal phenotype. This might imply a substantial difference in the biology of proximal and distal cancers, associated with different patterns of tumor cells dissemination. The poor prognosis of right-sided CRC is not determined by the hematogenous dissemination of tumor cells, which appears to be predominantly a passive shedding of non-viable cells. Conversely, the subgroup of poor-prognosis left-sided CRC is reliably identified by the presence of mesenchymal CTC. MDPI 2019-07-24 /pmc/articles/PMC6721440/ /pubmed/31344798 http://dx.doi.org/10.3390/cancers11081042 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nicolazzo, Chiara Raimondi, Cristina Gradilone, Angela Emiliani, Alessandra Zeuner, Ann Francescangeli, Federica Belardinilli, Francesca Seminara, Patrizia Loreni, Flavia Magri, Valentina Tomao, Silverio Gazzaniga, Paola Circulating Tumor Cells in Right- and Left-Sided Colorectal Cancer |
title | Circulating Tumor Cells in Right- and Left-Sided Colorectal Cancer |
title_full | Circulating Tumor Cells in Right- and Left-Sided Colorectal Cancer |
title_fullStr | Circulating Tumor Cells in Right- and Left-Sided Colorectal Cancer |
title_full_unstemmed | Circulating Tumor Cells in Right- and Left-Sided Colorectal Cancer |
title_short | Circulating Tumor Cells in Right- and Left-Sided Colorectal Cancer |
title_sort | circulating tumor cells in right- and left-sided colorectal cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721440/ https://www.ncbi.nlm.nih.gov/pubmed/31344798 http://dx.doi.org/10.3390/cancers11081042 |
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